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Cryoconservation de cellules souches d'embryons humains par un congélateur programmé avec un champ magnétique oscillant.

Cryopreservation of human embryonic stem cells by a programmed freezer with an oscillating magnetic field.

Auteurs : LIN P. Y., YANG Y. C., HUNG S. H., et al.

Type d'article : Article

Résumé

Human embryonic stem cells (hESCs),due to their self-renewal capacity and pluripotency, are an important source of cells for regenerative medicine. The immediate obstacles that need to be addressed are the poor cell survival rate of hESCs and their cell quality after cryopreservation. In this study, we used the Cell Alive System (CAS) which combines a programmed freezer with an oscillating magnetic field to reduce cryo-injur y during the freezing process. The hESC clumps suspended in freezing medium were divided into three groups: (i) cells frozen by a conventional freezing container, Mr. Frosty and kept in a -80°C freezer (MF); (ii) cells frozen to -32°C by CAS, and then transferred to a -80°C freezer (CAS); (iii) cells frozen to -32°C by CAS, and then transferred to a pre-cooled Mr. Frosty and kept in a -80°C freezer (CAS-MF) for overnight. All cryovials were placed in liquid nitrogen for one week, and hESCs were then thawed and cultured on feeder for 7days.The results of alkaline phosphatase (AP)staining showed that the attachment efficiency of the cells cryopreserved by CAS and CAS-MF was significantly higher (29.0% and 44.0%)than in the MF method (7.0%). Furthermore, we confirmed the cells cryopreserved using CAS- MF could be subcultured while expressing pluripotent markers, differentiate into three germ layers, and maintain a normal karyotype. These results demonstrate that the use of CAS-MF offers an efficient method of hESC banking.

Détails

  • Titre original : Cryopreservation of human embryonic stem cells by a programmed freezer with an oscillating magnetic field.
  • Identifiant de la fiche : 30013181
  • Langues : Anglais
  • Source : Cryobiology - vol. 66 - n. 3
  • Date d'édition : 06/2013
  • DOI : http://dx.doi.org/10.1016/j.cryobiol.2013.02.061

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